RS753296393 TNFRSF13B

Health Risk Chr 17:16939644
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Associated Conditions
Immunodeficiency
common variable
2
Inborn genetic diseases
Immunodeficiency
common variable
2
Inborn genetic diseases
Other Variants in TNFRSF13B
rs34557412 rs72553883 rs104894649 rs121908379 rs104894650 rs72553882 rs72553876 rs140781824 rs72553875 rs143027621
Ask Dr. Hemsworth about this variant